Tire sealant composition

ABSTRACT

Disclosed herein are a sealant composition for use with tires, a tire having at least one component with at least one surface at least partially coated with the sealant composition, and related methods for applying the sealant composition to tires. The sealant composition comprises biorubber and a softener comprising at least one of plant oil or plant resin and has a non-petroleum content of at least 70% by weight.

FIELD

The present application is directed to a sealant composition for usewith tires. Also disclosed are tires having at least one component withat least one surface at least partially coated with the sealantcomposition as well as related methods for applying the sealantcomposition to tires.

BACKGROUND

Sealant compositions may be used in pneumatic tires to improve aninstalled tire's durability when the vehicle upon which the tire isinstalled is operated. Use of the sealant composition may enable thepneumatic tire to withstand a puncture from a sharp object such as anail. By incorporating a sealant composition into an interior portion ofa pneumatic tire, one or more punctures which could otherwise render thevehicle inoperable or require repair can be plugged by flow or movementof the sealant composition into the hole created by the puncture.

SUMMARY

Disclosed herein are a sealant composition for use with tires, a tirehaving at least one component with at least one surface at leastpartially coated with the sealant composition, and related methods forapplying the sealant composition to tires.

In a first embodiment, a sealant composition for use with tires isdisclosed. The sealant composition comprises biorubber and a softenercomprising at least one of plant resin or plant oil, and optionally acure package, wherein the sealant composition contains at least 70weight % (based upon the total weight of the sealant composition)non-petroleum ingredients including the biorubber, and plant resin orplant oil, and the sealant composition has a viscosity of 200 to 500Pa-S at 100° C.

In a second embodiment, a tire comprising at least one component incontact with a sealant composition according to the first embodiment isdisclosed.

In a third embodiment, a method for applying a sealant composition to atire is disclosed. The method comprises: providing a tire comprising atleast one of the following components: a tread, one or more body orcarcass plies, one or more cap plies, one or more belt plies, asidewall, or an air barrier layer; and applying a sealant compositionaccording to the first embodiment to a portion of at least one radiallyinner surface of at least one of the components of the tire.

DETAILED DESCRIPTION

Disclosed herein are a sealant composition for use with tires, a tirehaving at least one component with at least one surface at leastpartially coated with the sealant composition, and related methods forapplying the sealant composition to tires.

In a first embodiment, a sealant composition for use with tires isdisclosed. The sealant composition comprises biorubber and a softenercomprising at least one of plant resin or plant oil, and optionally acure package, wherein the sealant composition contains at least 70weight % (based upon the total weight of the sealant composition)non-petroleum ingredients including the biorubber, and plant resin orplant oil, and the sealant composition has a viscosity of 200 to 500Pa-S at 100° C.

In a second embodiment, a tire comprising at least one component incontact with a sealant composition according to the first embodiment isdisclosed.

In a third embodiment, a method for applying a sealant composition to atire is disclosed. The method comprises: providing a tire comprising atleast one of the following components: a tread, one or more body orcarcass plies, one or more cap plies, one or more belt plies, asidewall, or an air barrier layer; and applying a sealant compositionaccording to the first embodiment to a portion of at least one radiallyinner surface of at least one of the components of the tire.

Definitions

As used herein, the term “majority” means 51% by weight or more.

As used herein, the term “natural rubber” or NR means naturallyoccurring rubber such as can be harvested from sources such as Hevearubber trees, and non-Hevea source (e.g., guayule shrubs, and dandelions(e.g., TKS)). In other words, the term “natural rubber” should not beconstrued as including polyisoprene.

As used herein, the term “polyisoprene” means synthetic polyisoprene. Inother words, the term is used to indicate a polymer that is manufacturedfrom isoprene monomers, and should not be construed as includingnaturally occurring natural rubber (e.g., Hevea natural rubber,guayule-sourced natural rubber or dandelion-sourced natural rubber). Theterm polyisoprene is also used interchangeably with the phrase“polyisoprene rubber” and the abbreviation “IR.”

For the purpose of the present disclosure, any reference to a percentamount of a component in the sealant composition means a percent byweight, unless otherwise specified. Similarly, any reference to ratiosof component amounts in the sealant composition means the ratios byweight, unless otherwise specified. Unless stated to the contrary,discussions herein relating to the components and amounts of the sealantcompositions of the present disclosure should be understood to applyequally to the other embodiments, e.g., the related methods and thetires containing the sealant compositions, as disclosed herein as thethird and second embodiments.

Sealant Composition

As discussed above, the first embodiment disclosed herein is directed toa sealant composition for use with tires. By stating that the sealantcomposition is for use with tires is meant that it is suitable for usewith various types of tires, especially pneumatic tires. The sealantcomposition according to the first embodiment may be consideredespecially suitable for acting as a plug in response to a puncture ofthe tire. As discussed above, the sealant composition of the firstembodiment can be utilized in the tire of the second embodiment and inthe method of the third embodiment. Thus, the various aspects of thesealant composition of the first embodiment as discussed herein andbelow should be understood as applying equally to the sealantcomposition utilized in the second and third embodiments describedherein. In other words, the various aspects of the sealant compositionof the first embodiment can be utilized in embodiments of the second andthird embodiments disclosed herein.

The sealant composition of the first embodiment comprises biorubber anda softener comprising at least one of plant resin or plant oil. One ormore than one biorubber can be utilized in the sealant compositions ofthe first embodiment. The softener component of the sealant compositionsof the first embodiment comprises at least one of plant resin or plantoil. In other words, the softener of the sealant compositions of thefirst embodiment comprises plant resin, plant oil, or a combinationthereof. In certain embodiments of the first embodiment, the softenercomponent of the sealant composition consists of plant resin, plant oil,or a combination thereof. When plant resin is utilized in an embodimentof the sealant composition, one or more than one plant resin, or one ormore than one source of plant resin may be utilized. When plant oil isutilized in an embodiment of the sealant composition, one or more thanone plant oil, or one or more than one source of plant oil may beutilized.

As discussed above, the sealant composition contains (comprises) atleast 70 weight % non-petroleum ingredients (based upon the total weightof the sealant composition) including the biorubber, and plant resinand/or plant oil. Non-petroleum ingredients are ingredients producedfrom sources other than petroleum products. For example, mostcommercially available styrene-butadiene rubbers are produced from1,3-butadiene and styrene monomers which have been sourced from(produced from) petroleum products. In contrast, a biorubber such asguayule natural rubber would be considered to be a non-petroleumingredient as would a biorubber produced from monomers made fromnon-petroleum ingredients (e.g., styrene made from cinnamic acid byyeast cells). According to the first embodiment at least the biorubberas well as any plant resin and plant oil present in the sealantcomposition contribute to the amount of non-petroleum ingredients. Incertain embodiments of the first embodiment, additional ingredients maycontribute to the amount of non-petroleum ingredients, e.g., certainfillers and/or various components of a cure package (when present). Incertain embodiments of the first embodiment, the sealant compositioncontains (comprises) at least 75 weight %, at least 80 weight %, atleast 85 weight %, at least 90 weight %, at least 95 weight %, at least98 weight %, at least 99 weight % or even 100 weight % non-petroleumingredients (based upon the total weight of the sealant composition).

As discussed above, according to the first embodiment disclosed herein,the sealant composition has a viscosity of 200 to 500 Pa*s (i.e., inunits of Pascal*seconds) at 100° C. Such viscosity refers to thekinematic or absolute viscosity of the sealant composition. One Pa*s isequivalent to 1 N s/m² (i.e., 1 Newton second/meter²) and alsoequivalent to 1 kg/(m/s) (i.e., 1 kilogram per (meters seconds).Kinematic viscosities can be determined by various methods includingASTM Method D6204 or ISO Method 13145. The viscosities referred toherein for the sealant composition are intended to refer to viscositiesmeasured using the method discussed in the working examples (which isbased upon ASTM Method D6204) or an equivalent method, and as measuredat 100° C. In certain embodiments of the first embodiment disclosedherein, the sealant composition has a viscosity of about 200 to about500 Pa*s at 100° C., 200 to 500 (e.g., 200, 210, 220, 230, 240, 250,260, 270, 280, 290, 300, 310, 320, 330, 340, 350, 360, 370, 380, 390,400, 410, 420, 430, 440, 450, 460, 470, 480, 490, 500) Pa*s at 100° C.,about 250 to about 500 Pa*s at 100° C., 250 to 500 Pa*s at 100° C.,about 250 to about 450 Pa*s at 100° C., 250 to 450 Pa*s at 100° C.,about 260 to about 450 Pa*s at 100° C., 260 to 450 Pa*s at 100° C.,about 270 to about 450 Pa*s at 100° C., 270 to 450 Pa*s at 100° C.,about 280 to about 450 Pa*s at 100° C., 280 to 450 Pa*s at 100° C.,about 290 to about 450 Pa*s at 100° C., 290 to 450 Pa*s at 100° C.,about 300 to about 450 Pa*s at 100° C., 300 to 450 Pa*s at 100° C.,about 310 to about 450 Pa*s at 100° C., 310 to 450 Pa*s at 100° C.,about 320 to about 450 Pa*s at 100° C., 320 to 450 Pa*s at 100° C.,about 250 to about 440 Pa*s at 100° C., 250 to 440 Pa*s at 100° C.,about 250 to about 430 Pa*s at 100° C., 250 to 430 Pa*s at 100° C.,about 250 to about 420 Pa*s at 100° C., 250 to 420 Pa*s at 100° C.,about 250 to about 410 Pa*s at 100° C., 250 to 410 Pa*s at 100° C.,about 250 to about 400 Pa*s at 100° C., or 250 to 400 Pa*s at 100° C. Incertain preferred embodiments of the first embodiment, the sealantcomposition has a viscosity of 300 to 450 Pa*s at 100° C., or 300 to 400Pa*s at 100° C.

In certain embodiments of the first embodiment, the sealant compositionwill remain tacky (at room temperature, 25° C.) even after any curingsuch that an object (such as a coin) dropped onto the sealantcomposition from a height of 12 inches will stick sufficiently to thesurface of the sealant composition that tipping or turning upside downwill not dislodge the object. In certain embodiments of the firstembodiment, the tackiness of the sealant composition (at roomtemperature) is at least 1000 Newtons as measured by a strain gaugeusing the following test. A nail is driven into a sample of rubber tirethat has been coated on its interior surface with sealant composition,preferably the nail is driven until its head rests against the outersurface of the tire and the end of the nail passes into (and optionallyentirely through) the sealant composition. Thereafter, the forcerequired to remove the nail from the tire is measured (in Newtons) witha strain gauge. Higher force measurements are indicative of highertackiness in the sealant composition. In certain embodiments of thefirst embodiment, the tackiness of the sealant composition (at roomtemperature) is about 800 to about 3000 (e.g., 800, 900, 1000, 1100,1200, 1300, 1400, 1500, 1600, 1700, 1800, 1900, 2000, 2100, 2200, 2300,2400, 2500, 2600, 2700, 2800, 2900, 3000) Newtons (as measured by astrain gauge using the preceding test), including 800-3000 Newtons,about 800 to about 2500 Newtons, 800-2500 Newtons, about 800 to about1500 Newtons, 800-1500 Newtons, about 900 to about 3000 Newtons,900-3000 Newtons, about 900 to about 2500 Newtons, 900-2500 Newtons,about 900 to about 1500 Newtons, or 900-1500 Newtons. Alternatively,tackiness can be measured by various methods, including ASTM MethodD2979. It should be understood that the foregoing tackiness descriptionsincluding the ranges provided apply equally to certain embodiments ofthe second embodiment (e.g., in describing suitable sealant compositionsfor use on a tire component) and to certain embodiments of the thirdembodiment (e.g., in describing suitable sealant compositions for use inthe method of the third embodiment).

The relative amounts of biorubber and softener utilized in the sealantcompositions according to the first embodiment disclosed herein mayvary. In certain embodiments of the first embodiment, the biorubber ispresent in an amount of about 15 to about 90 weight % (based upon thetotal weight of the sealant composition), including 15 to 90% (e.g., 15,20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, or 90%) byweight, about 20 to about 85% by weight, 20 to 85% by weight, about 25to about 85% by weight, 25 to 85% by weight, about 30 to about 85% byweight, 30 to 85% by weight, about 20 to about 80% by weight, 20 to 80%by weight, about 25 to about 80% by weight, 25 to 80% by weight, about30 to about 80% by weight, 30 to 80% by weight, about 20 to about 75% byweight, 20 to 75% by weight, about 25 to about 75% by weight, 25 to 75%by weight, about 30 to about 75% by weight, 30 to 75% by weight, about20 to about 70% by weight, 20 to 70% by weight, about 25 to about 70% byweight, 25 to 70% by weight, about 30 to about 70% by weight, 30 to 70%by weight, about 20 to about 65% by weight, 20 to 65% by weight, about25 to about 65% by weight, 25 to 65% by weight, about 30 to about 65% byweight, 30 to 65% by weight, about 20 to about 60% by weight, 20 to 60%by weight, about 25 to about 60% by weight, 25 to 60% by weight, about30 to about 60% by weight, 30 to 60% by weight, about 20 to about 55% byweight, 20 to 55% by weight, about 25 to about 55% by weight, 25 to 55%by weight, about 30 to about 55% by weight, 30 to 55% by weight, about20 to about 51% by weight, 20 to 51% by weight, about 25 to about 51% byweight, 25 to 51% by weight, about 30 to about 51% by weight, 30 to 51%by weight, about 20 to about 50% by weight, 20 to 50% by weight, about25 to about 50% by weight, 25 to 50% by weight, about 30 to about 50% byweight, 30 to 50% by weight, about 35 to about 90% by weight, 35 to 90%by weight, about 40 to about 90% by weight, 40 to 90% by weight, about45 to about 90% by weight, 45 to 90% by weight, about 50 to about 90% byweight, 50 to 90% by weight, about 51 to about 90% by weight, or 51 to90% by weight. When more than one biorubber is present, the foregoingranges should be understood to refer to the total amount of allbiorubbers. In those embodiments of the first embodiment wherein thebiorubber of the sealant composition has a lower Mw (e.g., 175,000 orless), the amount of biorubber may preferably be somewhat larger such asabout 30 to about 90% by weight (30 to 90% by weight) or even about 40to about 80% by weight (40 to 80% by weight) to accord for less oilbeing used in the overall sealant composition; the foregoing rangesshould be understood to include intermediary ranges and amounts, e.g.,30 to 90 includes 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, and 90and 40 to 80 includes 40, 45, 50, 55, 60, 65, 70, 75, and 80. In certainembodiments of the first embodiment, the softener of the sealantcomposition is present in an amount of about 10 to about 85 weight %(based upon the total weight of the sealant composition), including 10to 85 weight %, about 10 to about 80 weight %, 10 to 80 weight %, about10 to about 75 weight %, 10 to 75 weight %, about 10 to about 70 weight%, 10 to 70 weight %, about 10 to about 65 weight %, 10 to 65 weight %,about 10 to about 60 weight %, 10 to 60 weight %, about 10 to about 55weight %, 10 to 55 weight %, about 10 to about 50 weight %, 10 to 50weight %, about 15 to about 85 weight %, 15 to 85 weight %, about 15 toabout 80 weight %, 15 to 80 weight %, about 15 to about 75 weight %, 15to 75 weight %, about 15 to about 70 weight %, 15 to 70 weight %, about20 to about 85 weight %, 20 to 85 weight %, about 20 to about 80 weight%, 20 to 80 weight %, about 20 to about 75 weight %, 20 to 75 weight %,about 20 to about 70 weight %, 20 to 70 weight %, about 25 to about 70weight %, 25 to 70 weight %, about 30 to about 85 weight %, 30 to 85weight %, about 30 to about 80 weight %, 30 to 80 weight %, about 30 toabout 85 weight %, 30 to 85 weight %, about 30 to about 70 weight %, 30to 70 weight %, about 35 to about 70 weight %, or 35 to 70 weight %. Inthose embodiments of the first embodiment wherein the biorubber of thesealant composition has a lower Mw (e.g., 175,000 or less), the amountof biorubber may preferably be somewhat larger (as discussed above), andaccordingly the amount of softener may be somewhat lower such as about10 to about 85% by weight (10 to 85% by weight) or even about 15 toabout 50% by weight (15 to 50% by weight) to accord for less oil beingused in the overall sealant composition; the foregoing ranges should beunderstood to include intermediary ranges and amounts, e.g., 10 to 85includes 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80 and85 and 15 to 50 includes 15, 20, 25, 30, 35, 40, 45, and 50.

In certain embodiments of the first embodiment, the sealant compositionconsists of biorubber and a softener either comprising or consisting ofa plant resin. In certain embodiments of the first embodiment, thesealant composition consists of biorubber and a softener eithercomprising or consisting of a plant oil. In certain embodiments of thefirst embodiment, the sealant composition consists of biorubber and asoftener either comprising or consisting of: a plant resin, a plant oilor a combination thereof. In certain embodiments of the firstembodiment, the softener of the sealant composition either comprises orconsists of a plant resin which is present in an amount of about 10 toabout 45 weight % (based upon the total weight of the sealantcomposition), including 10 to 45 weight %, about 10 to about 40% byweight, 10 to 40% by weight, about 10 to about 35% by weight, 10 to 35%by weight, about 10 to about 30% by weight, 10 to 30% by weight, about15 to about 45% by weight, 15 to 45% by weight, about 20 to about 45% byweight, 20 to 45% by weight, about 25 to about 45% by weight, or 25 to45% by weight; in certain embodiments of the foregoing, thebiorubber:plant resin weight ratio is greater than 1:1 (i.e., relativelymore biorubber than plant resin is present in the sealant composition ona weight basis).

Biorubber

As discussed above, the sealant composition of the first-thirdembodiments comprises (includes) biorubber. One or more than onebiorubber may be utilized. As used herein, the term biorubber isintended to refer to a rubber that has a modern carbon content of50-100%. As those of skill in the art will appreciate, petroleum-basedhydrocarbons are sourced from fossil fuels or other petroleum products,which by their nature, do not contain any “modern” carbon. Moderncarbon, as used herein, refers to the standard set forth in ASTM D6866.Generally speaking, under this standard, modern carbon contains the same¹⁴C activity level (including the post-1950 correction) as the originaloxalic acid radiocarbon carbon that occurs naturally and is found inplants and animals at approximately the same concentration found in theatmosphere. Due to radioactive decay, fossil fuels lack any measurable¹⁴C activity, and, therefore, do not contain any modern carbon, andaccordingly, petroleum-based hydrocarbons made from those fossil fuelsalso do not contain any modern carbon. Non-petroleum ingredients,including the biorubbers (and plant resins and plant oils) disclosedherein, will display ¹⁴C activity, and therefore will contain moderncarbon. In certain embodiments of the first-third embodiments, suitablebiorubbers may have a modern carbon content of at least 50%, at least60%, at least 70%, at least 75%, at least 80%, at least 85%, at least90%, at least 95%, at least 98% or even 100%, including 50-100%, 50-98%,50-95%, 50-90%, 50-85%, 50-80%, 50-75%, 50-70%, 50-60%, 60-100%, 60-98%,60-95%, 60-90%, 60-85%, 60-80%, 60-75%, 60-70%, 70-100%, 70-98%, 70-95%,70-90%, 70-85%, 70-80%, 70-75%, 75-100%, 75-98%, 75-95%, 75-90%, 75-85%,75-80%, 80-100%, 80-98%, 80-95%, 80-90%, 80-85%, 85-100%, 85-98%,85-95%, 85-90%, 90-100%, 90-98%, and 90-95%.

In certain embodiments of the first-third embodiments disclosed herein,the biorubbers may be produced as a polymer or rubber from a plant(e.g., Hevea natural rubber or non-Hevea natural rubber such as sourcedfrom guayule or dandelion), polymerized from one or more biomonomers, orconstitute a combination of the foregoing. In certain embodiments of thefirst-third embodiments disclosed herein, the biorubber comprises atleast one of: polyfarnesene, non-Hevea natural rubber, Hevea naturalrubber, or a polymer or copolymer comprising at least one conjugateddiene-containing non-petroleum monomer optionally in combination with atleast one aromatic vinyl non-petroleum monomer. In certain embodimentsof the first-third embodiments disclosed herein, the biorubber comprisesat least one of: polyfarnesene, non-Hevea natural rubber, Hevea naturalrubber, styrene-butadiene rubber, polybutadiene rubber, polyisoprenerubber, styrene-isoprene rubber, styrene-butadiene-isoprene rubber,ethylene propylene diene monomer rubber (also known as EPDM rubber),butyl rubber, or halogenated butyl rubber (e.g., bromobutyl andchlorobutyl rubber). As used herein the term butyl rubber refers to acopolymer of isobutylene and a small amount of a diene-based monomer,typically isoprene or para-methylstyrene. In certain embodiments of thefirst-third embodiments disclosed herein, the biorubber consists of(i.e., no other rubbers are contained in the sealant compositionaccording to such embodiments) one or more of the following:polyfarnesene, non-Hevea natural rubber, Hevea natural rubber,styrene-butadiene rubber, polybutadiene rubber, polyisoprene rubber,styrene-isoprene rubber, styrene-butadiene-isoprene rubber, ethylenepropylene diene monomer rubber (also known as EPDM rubber), butylrubber, or halogenated butyl rubber. In certain embodiments of thefirst-third embodiments disclosed herein, the biorubber comprisespolyfarnesene. In certain embodiments of the first-third embodimentsdisclosed herein the polyfarnesene biorubber is produced from monomersof beta-farnesene (which is not only branched but contains a conjugateddiene bond). In certain embodiments of the first-third embodimentsdisclosed herein, at least 90% by weight of the biorubber has a Mw(determined by GPC using a polystyrene standard) of 175,000 or less; incertain such embodiments of the first-third embodiments, at least 95%,at least 98%, or even 100% of the biorubber has a Mw of 175,000 or less.In certain embodiments of the first-third embodiments disclosed herein,the polyfarnesene biorubber has a molecular weight (Mw) of up to about500,000 kDa (e.g., 500,000; 400,000, 350,000; 300,000; 250,000; 200,000;150,000; 175,000, 100,000 all in kDa), including up to 500,000 kDa; upto about 400,000 kDa; up to 400,000 kDa; up to about 300,000 kDa; up to300,000 kDa; up to about 200,000; up to 200,000; up to about 175,000; upto 175,000; about 100,000 to about 500,000 kDa; about 100,000 kDa to500,000 kDa; about 100,000 to about 300,000 kDa; 100,000 to 300,000 kDa;about 100,000 to about 200,000 kDa; and 100,000 to 200,000 kDa, all asdetermined by GPC (using a polystyrene standard). In certain embodimentsof the first-third embodiments disclosed herein, the biorubber comprisesat least one of Hevea rubber or non-Hevea rubber having a molecularweight (Mw) of up to about 2 million grams/mole, including up to 2million grams/mole (e.g., 2 million, 1.75 million, 1.5 million, 1.25million, 1 million, 0.75 million, 0.5 million, and less), up to 1.5million, up to 1 million, 0.5 million to 2 million, 0.75 million to 2million, 0.5 million to 1.75 million, and 0.75 million to 1.75 million,all using a light scattering method. In certain embodiments of thefirst-third embodiments disclosed herein, the biorubber comprisesnon-Hevea natural rubber. In certain embodiments of the first-thirdembodiments, the biorubber comprises no more than 25%, no more than 15%,no more than 10%, no more than 5%, or 0% by weight Hevea natural rubber.In certain embodiments of the first-third embodiments, the sealantcomposition comprises no more than 25%, no more than 15%, no more than10%, no more than 5% or 0% by weight Hevea natural rubber. In certainembodiments of the first-third embodiments, the biorubber comprises nomore than 25%, no more than 15%, no more than 10%, no more than 5%, or0% by weight EPDM rubber. In certain embodiments of the first-thirdembodiments, the biorubber comprises no more than 25%, no more than 15%,no more than 10%, no more than 5%, or 0% by weight butyl rubber. Incertain embodiments of the first-third embodiments disclosed herein, thebiorubber comprises at least one polymer or copolymer comprising atleast one conjugated diene-containing non-petroleum monomer optionallyin combination with at least one aromatic vinyl non-petroleum monomer.The amounts and ranges of biorubber discussed above should be understoodto apply to the particular polymers and polymers described herein thatmay constitute the biorubber. In certain embodiments of the first-thirdembodiments, the sealant composition comprises no more than 25% byweight of an elastomer that is solid at room temperature (based upon thetotal weight of the sealant composition); in certain of theseembodiments, the amount of elastomer that is solid at room temperatureis no more than 20%, no more than 15%, no more than 10%, or no more than5% by weight (based upon the total weight of the sealant composition).

As those of skill in the art understand, a conjugated diene is acompound that has two double carbon-carbon bonds (i.e., two —C═C— bonds)that are separated by a single bond (i.e., —C—C—); a conjugated dienewill contain at least one —C═C—C═C— moiety). The particular structure ofthe conjugated diene monomer used in the embodiments of the first-thirdembodiments disclosed herein can vary. Non-limiting examples of suitableconjugated diene monomers according to certain embodiments of thefirst-third embodiments disclosed herein include, but are not limitedto, 1,3-butadiene, isoprene, 1,3-pentadiene, 1,3-hexadiene,2,3-dimethyl-1,3-butadiene, 2-ethyl-1,3-butadiene,2-methyl-1,3-pentadiene, 3-methyl-1,3-pentadiene,4-methyl-1,3-pentadiene, 2,4-hexadiene, 1,3-cyclopentadiene,1,3-cyclohexadiene, 1,3-cycloheptadiene, and 1,3-cyclooctadiene, andderivatives thereof. It should be understood that mixtures of two ormore conjugated diener may be utilized in certain embodiments. Incertain embodiments of the first-third embodiments, the conjugated dienemonomer comprises 1,3-butadiene. In certain embodiments of thefirst-third embodiments disclosed herein, the conjugated dienemonomer-containing polymer or copolymer is a copolymer which furthercomprises at least one vinyl aromatic monomer) (i.e., in addition to theconjugated diene monomer). In certain embodiments of the first-thirdembodiments disclosed herein, the at least one vinyl aromatic monomercomprises at least one of styrene, alpha-methyl styrene,p-methylstyrene, o-methylstyrene, p-butylstyrene, vinylnaphthalene,p-tertbutylstyrene, 4-vinylbiphenyl, 4-vinylbenzocyclobutene,2-vinylnaphthalene, 9-vinylanthracene, 4-vinylanisole, or vinylcatechol. In certain embodiments of the first-third embodimentsdisclosed herein, the at least one vinyl aromatic monomer comprisesstyrene. In certain embodiments of the first-third embodiments disclosedherein, the at least one conjugated diene monomer comprises1,3-butadiene and the at least one vinyl aromatic monomer comprisesstyrene. In certain embodiments of the first-third embodiments disclosedherein, the biorubber comprises a copolymer of isobutylene and a dienemonomer (e.g., isoprene or paramethyl styrene).

Various non-petroleum sources of the monomers, polymers and copolymersdiscussed above exist. As non-limiting examples, polyfarnesene producedfrom the fermentation of sugarcane can be purchased from Kuraray Co.,Ltd. or its U.S.-affiliate Kuraray America Inc. and guayule naturalrubber is available from Yulex Corporation (San Diego, Calif.) such asunder the product name Yulex Pure™. Isoprene monomers suitable forproducing biorubbers can be produced from biobased butanols, pentanols,and combinations, thereof, which can be obtained by thermochemical orfermentation processing of biomass. An exemplary process for convertingthese biobased alcohols to bioisoprene is described in U.S. PatentApplication Publication No. 2010/0216958, the contents of which areincorporated herein by reference. Alternatively, examples of a biobasedisoprene source include carbohydrates, glycerol, glycerine,dihydroxyacetone, single-carbon sources, animal fat, animal oils, fattyacids, lipids, phospholipids, glycerolipids, monoglycerides,diglycerides, triglycerides, polypeptides, yeast extracts, andcombinations thereof. An exemplary process for converting these biobasedsources to isoprene is described in U.S. Patent Application PublicationNo. 2011/0237769, the contents of which are incorporated herein byreference. Styrene monomers suitable for producing biorubbers can beproduced from ingredients such as cinnamic acid, derivatives of cinnamicacid, syngas (i.e., biobased syngas such as syngas from biomass),methane (i.e., biobased methane such as methane from biomass), ethanol,butanol, and combinations thereof. Cinnamic acid can be obtained fromcinnamon oil; resinous exudates from balsam trees, e.g., storax; fatextracts from shea trees, e.g., shea butter; and deamination ofL-phenylalanine made from biomass. Biobased derivatives of cinnamicacid, such as hydrocinnamic acid, are, as their name implies, derivedfrom biobased cinnamic acid. Biobased hydrocinnamic acid can be obtainedby hydrogenating biobased cinnamic acid. Biobased syngas, whichtypically contains hydrogen, carbon monoxide, and carbon dioxide, can beobtained through the gasification of biomass. Biobased methane can beproduced by the catalytic conversion of a biobased syngas. Biobasedbutanol and biobased ethanol, can be produced by the fermentation ofbiomass. For example, each of butanol and ethanol can be produced by theacetone-butanol-ethanol method of fermentation, which is the bacterialfermentation of carbohydrates such as starch in the absence of oxygen.Biobased ethanol can also be produced from yeast fermentation ofcarbohydrates such as cellulose. Non-Hevea sources of natural rubberinclude, but are not limited to, Parthenium argentatum (Guayule shrub),Taraxacum Kok-Saghyz (Russian dandelion), Euphorbia lathyris (gopherplant), Parthenium incanum (mariola), Chrysothamnus nauseosus(rabbitbrush), Pedilanthus macrocarpus (candililla), Asclepias syriaca,speciosa, subulata, et al (milkweeds), Solidago altissima, graminifoliarigida, et al (goldenrods), Cacalia atripilicifolia (pale Indianplantain), Pycnanthemum incanum (mountain mint), Teucreum canadense(American germander) and Campanula Americana (tall bellflower). Incertain embodiments of the first-third embodiments disclosed herein, thebiorubber is sourced from one or more of the foregoing plants. Incertain embodiments of the first-third embodiments disclosed herein, thebiorubber is sourced from at least one of Parthenium argentatum (Guayuleshrub) or Taraxacum Kok-Saghyz (Russian dandelion). In certainembodiments of the first-third embodiments disclosed herein, thebiorubber is sourced from Parthenium argentatum (Guayule shrub);according to such embodiments such biorubber may alternatively bedescribed as guayule natural rubber. Other plants which produce rubberand rubber-like hydrocarbons are known, particularly among theCompositae, Euphorbiaceae, Campanulaceae, Labiatae, and Moraceafamilies.

In certain embodiments of the first-third embodiments disclosed herein,the biorubber is extended with at least a portion of the plant resinand/or plant oil. By extended with is meant that the biorubber containsat least a portion of the plant resin, at least a portion of the plantoil, or at least a portion of plant resin and plant oil that iscontained in the overall sealant composition. In certain embodiments ofthe first-third embodiments disclosed herein, the biorubber is extendedwith at least a portion of the plant resin, at least a portion of theplant oil, or at least a portion of both by pre-mixing the biorubberwith a quantity of plant resin, plant oil or both. In certainembodiments of the first-third embodiments disclosed herein, thebiorubber is extended with at least a portion of the plant resin as aresult of an inherent amount of plant resin being contained with theplant source of the biorubber; in certain such embodiments the amount ofplant resin in the biorubber comprises up to 10% (e.g., 10%, 9%, 8%, 7%,6%, 5%, 4%, 3%, 2%, 1%, or less than 1%), including 0.01 to 10% byweight of the biorubber. A non-limiting example of a biorubber extendedwith at least a portion of the plant resin as a result of the foregoingis guayule rubber; in certain such embodiments, the biorubber comprisesguayule rubber containing about 1 to about 10% by weight guayule resin,including 1-10% (e.g., 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%. 9%, or 10%),about 1 to about 7%, 1-7%, about 1 to about 5%, or 1-5% guayule resin.Other examples of biorubbers extended with at least a portion of plantresin from inherent sources of the plant resin include non-Hevea naturalrubber from Russian dandelion and Hevea natural rubber which may containup to about 2% resin, including up to 2% resin, up to about 1.5% resin,up to 1.5% resin, up to about 1% resin, or up to 1% resin (all of theforegoing by weight).

Softener

As discussed above, the sealant composition of the first-thirdembodiments comprises (includes) a softener which comprises at least oneof plant resin or plant oil. In certain embodiments of the first-thirdembodiments, the softener comprises at least one plant resin. In certainembodiments of the first-third embodiments, the softener consists of atleast one plant resin. In certain embodiments of the first-thirdembodiments, the softener comprises at least one plant oil. In certainembodiments of the first-third embodiments, the softener consists of atleast one plant oil. In certain embodiments of the first-thirdembodiments, the softener consists of at least one plant resin and atleast one plant oil.

As used herein, the phrase “plant resin” refers to resins sourced fromone or more plants. Such resins are generally viscous (often highlyviscous at room temperature) liquids that are insoluble in water. Incertain embodiments of the first-third embodiments disclosed herein, theplant resin meets at least one of the following: contains at least amajority by weight of one or more terpenes, or has the property ofhardening into a solid after some period of exposure to air (usuallymeasured in days or weeks). As used herein, plant resins are notintended to encompass petroleum resins such as C5 aliphatic and C9aromatic resins (usually obtained as a by-product of petroleumcracking). Various plant sources of plant resins exist includingguayule, conifer, and citrus (e.g., lemon, lime, orange), any of whichcan be utilized in certain embodiments of the first-third embodimentsdisclosed herein. Plant resins used in the first-third embodimentsdisclosed herein may comprise (include) a combination of various typesof compounds. In addition to the terpene compounds that comprise theplant resins, other compounds present include, but are not limited to,argentatins and guayulins. In certain embodiments of the first-thirdembodiments disclosed herein, the plant resin comprises (includes) atleast one terpene, at least one argentatin, at least one guayulin, or acombination thereof. Most plant resins will contain both a volatile andnon-volatile fraction. In certain embodiments of the first-thirdembodiments, the volatile fraction may comprise mostly various terpenecompounds. The non-volatile fraction may include one or more of: fattyacids (i.e., free fatty acids), argentatins, guayulins, aldehydes, andalcohols. In certain embodiments of the first-third embodiments, theplant resin comprises at least one of (1)-(6) as follows: (1) at leastone terpene selected from d-limonene, limonene, alpha-pinene,beta-pinene, d-verbenone, camphene, alpha-thugene, beta-myrcene,delta-3-carene, terpinolene, beta-ocimene, or santolina triene; (2) atleast one fatty acid selected from: cinnamic acid, alpha-linoleic acid,beta-linoleic acid, stearic acid, palmitic acid, palmitoleic acid, oroleic acid; (3) at least one argentatin selected from Argentatin A,Argentatin B, or Argentarin C; (4) at least one guayulin selected fromGuayulin A, or Guayulin B; (5) at least one fatty acid (as free fattyacid, monoglyceride, diglyceride, triglyceride, or a combinationthereof) selected from linoleic acid, cinnamic acid, linolenic acid,palmitic acid, oleic acid, p-anisic acid, or stearic acid; or (6) lowmolecular weight polyisoprene rubber having a degree of polymerizationof less than 400. In certain embodiments of the first-third embodiments,when at least one fatty acid is present, at least a majority of thefatty acids comprises a combination of linoleic, cinnamic, linolenic andpalmitic acids. It should be understood that either anaturally-occurring plant resin, a processed plant resin, or both can beutilized in certain embodiments of the first-third embodiments;processed forms of plant resins may contain more or less of certaincompounds than their naturally-occurring counterparts. In certainembodiments of the first-third embodiments, the plant resin comprisesguayule resin, optionally meeting at least one of the foregoing (1)-(6).In certain embodiments of the first-third embodiments, the plant resincomprises guayule resin wherein at least 40 weight % of the guayuleresin comprises a combination of: terpenes and sesquiterpenes, GuayulinA, Guayulin B, cinnamate C, anisate D, Argentatin A, Argentatin B,Argentatin C, triterpenoid D, sterol glycosides, phytosterols andtriterpenoids, and fatty acids (as free fatty acid, monoglycerides,diglycerides, triglycerides, or a combination thereof). In certainembodiments of the first-third embodiments, the plant resin comprises apolymerized citrus resin (e.g., polylimonene, polyterpene, etc.); incertain such embodiments, the polymerized citrus resin may be a solid atroom temperature. In certain embodiments of the first-third embodiments,the volatile fraction of the plant resin is about 15 to about 30% byweight (based upon the total weight of the plant resin), including15-30% by weight, 15-25% by weight, and 17-22% by weight; in certainsuch embodiments the plant resin comprises guayule resin. In certainembodiments of the first-third embodiments, the plant resin comprisesabout 15 to about 35% by weight (based upon the total weight of theplant resin) of one or more argentatins, including 15-35% by weight,15-30% by weight, and 17-27% by weight; in certain such embodiments theplant resin comprises guayule resin. In certain embodiments of thefirst-third embodiments, the plant resin comprises about 10-25% byweight (based upon the total weight of the plant resin) of one or morefatty acids (as free fatty acid, monoglyceride, diglyceride,triglyceride, or a combination thereof), including 10-20% by weight, and12-17% by weight; in certain such embodiments the plant resin comprisesguayule resin.

As used herein, the phrase “plant oil” is intended to refer toingredients sourced from one or more plants which contain at least amajority by weight of one or more triglycerides, one or morediglycerides, one or more monoglycerides, or a combination thereof. Atriglyceride is an ester having a glycerol backbone with three fattyacids bonded thereto whereas a diglyceride has two fatty acids bondedthereto and a monoglyceride has one fatty acid bonded thereto. As usedherein, plant oils are not intended to encompass mineral oils orpetroleum oils (e.g., paraffinic oil, aromatic oil, naphthenic oil, TRAEoil, TDAE oil, MES oil). In certain embodiments of the first-thirdembodiments, the plant oil comprises at least 70% by weight of one ormore triglycerides, one or more diglycerides, one or moremonoglycerides, or a combination thereof. In certain embodiments of thefirst-third embodiments disclosed herein, the plant oil comprises atleast 75%, at least 80%, at least 85%, at least 90%, at least 95%, atleast 98%, at least 99% or even 100% by weight of one or moretriglycerides, one or more diglycerides, one or more monoglycerides, ora combination thereof; in certain such embodiments the foregoing amountsare comprised of one or more triglycerides in combination with one ormore diglycerides. In certain embodiments of the first-third embodimentsdisclosed herein, the plant oil comprises no more than 15%, no more than10%, no more than 8%, no more than 5%, no more than 3%, no more than 2%,no more than 1%, or even 0% by weight of free fatty acids andmonoglycerides (with the foregoing amounts referring to a total of allfree fatty acids and diglycerides present in such plant oil). In certainembodiments of the first-third embodiments disclosed herein, thesoftener composition comprises no more than 10%, no more than 5%, nomore than 3%, no more than 2%, no more than 1%, or even 0% by weight ofany petroleum oil.

In those embodiments of the first-third embodiments disclosed herein,where the softener comprises (includes) one or more plant oils, theplant source of the oil(s) may vary and may comprises one or more thanone plant. Various plant sources of plant oils exist including grains,nuts and vegetables, any of which can be utilized in certain embodimentsof the first-third embodiments disclosed herein. In certain embodimentsof the first-third embodiments disclosed herein, the softener comprises(includes) at least one of the following plant oils: soybean oil, palmoil, rapeseed oil, sunflower oil, peanut oil, cottonseed oil, oilproduced from palm kernel, coconut oil, olive oil, corn oil, grape seedoil, hazelnut oil, hemp oil, linseed oil, rice oil, safflower oil,sesame oil, mustard oil, or flax oil. In certain embodiments of thefirst-third embodiments disclosed herein, the softener comprises acombination of plant oils such as more than one of the foregoing plantoil; such a combination of plant oils is sometimes called a vegetableoil. In certain embodiments of the first-third embodiments disclosedherein, the softener comprises (includes) soybean oil. In certainembodiments of the first-third embodiments disclosed herein, thesoftener comprises (includes) sunflower oil; in certain suchembodiments, the sunflower oil comprises high-oleic sunflower oil (e.g.,having an oleic acid content of at least 60%, at least 70%, or at least80% by weight oleic acid). In certain embodiments of the first-thirdembodiments, oil is present in the sealant composition and the oilcomprises 10-70% by weight (e.g., 10%, 15%, 20%, 25%, 30%, 35%, 40%,45%, 50%, 55%, 60%, 65%, 70%) of the sealant composition; in certainsuch embodiments, the amount of oil in the sealant composition is nomore than 25% by weight of the sealant composition, no more than 20% byweight of the sealant composition, no more than 15% by weight of thesealant composition, no more than 10% by weight of the sealantcomposition, or no more than 5% by weight of the sealant composition.

According to the embodiments of the first-third embodiments disclosedherein, the relative amounts of plant resin and plant oil used as thesoftener component can vary. In certain embodiments of the first-thirdembodiments, the amount of plant resin is about 5 to about 100% byweight of the softener, including 5 to 100% by weight (e.g., 5, 10, 15,20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 98, or100% by weight) and the amount of plant oil is 0 to about 95% by weightof the softener, including 0 to 95% by weight (e.g., 0, 5, 10, 15, 20,25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, or 95% byweight). When more than one biorubber is used in the sealant compositionof the first-third embodiments, the foregoing amounts and ranges shouldbe understood to refer to the total amount of all biorubbers. In certainembodiments of the first-third embodiments wherein at least 90% of thebiorubber has a Mw of 175,000 or less (as discussed above), the relativeamount of plant oil as compared to plant resin in the softener may besomewhat less such as about 75 to 100% by weight of the softener,including 75 to 100% by weight (e.g., 75, 80, 85, 90, 95, 98, or 100% byweight) and the relative amount of plant resin may be somewhat more such0 to about 25% by weight of the softener, including 0 to 25% by weight(e.g., 0, 5, 10, 15, 20, or 25% by weight). When more than one plant oiland/or more than one plant resin is used for the softener of the sealantcomposition of the first-third embodiments, the foregoing amounts andranges should be understood to refer to the total amount of all plantresins and the total amount of all plant oils.

Filler

In certain embodiments of the first-third embodiments disclosed herein,the sealant composition further comprises (includes) at least onefiller. In certain such embodiments, the at least one filler is presentin an amount of up to 20 weight % (based upon the total weight of thesealant composition). In certain embodiments of the first-thirdembodiments disclosed herein, the sealer composition comprises at leastone filler in an amount of about 1 to 20 weight %, including 1 to 20weight % (e.g., 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%,14%, 15%, 16%, 17%, 18%, 19%, 20%), 1-15 weight %, 1-10 weight %, 1-8weight %, 1-5 weight %, 2-15 weight %, 2-10 weight %, 2-8 weight %, 2-5weight %, 3-15 weight %, 3-10 weight %, 3-8 weight %, 3-5 weight %, 5-15weight %, 5-10 weight %, or 5-8 weight %. One or more than one fillermay be utilized. In certain embodiments of the first-third embodimentsthe at least one filler can include: at least one reinforcing filler, atleast one non-reinforcing filler, or a combination thereof. In certainembodiments of the first-third embodiments disclosed herein, the atleast one filler is present in an amount based upon 100 parts ofbiorubber such as about 1 to about 40 phr or 1-40 phr filler (i.e.,parts per 100 parts of biorubber), preferably 5 to about 25 phr or 5-25phr filler.

As used herein, the term “non-reinforcing filler” is used to refer to aparticulate material that has a nitrogen absorption specific surfacearea (N₂SA) of less than about 20 m²/g (including less than 20 m²/g),and in certain embodiments less than about 10 m²/g (including less than10 m²/g). The N₂SA surface area of a particulate material can bedetermined according to various standard methods including ASTM MethodD6556 (as of the time of filing this application most recently issued asD6556-14 in 2014) or ASTM Method D1993 for silica fillers (as of thetime of filing this application most recently issued as D1993-03(reapproved in 2013)), each of which are B.E.T. nitrogen absorptionmethods. Additionally or alternatively, the term “non-reinforcingfiller” is used to refer to a particulate material that has a particlesize of greater than about 1000 nm (including greater than 1000 nm). Asused herein, the term “reinforcing filler” is used to refer to aparticulate material that has a nitrogen absorption specific surfacearea (N₂SA) of about 20 m²/g or greater, including 20 m²/g or greater,more than about 50 m²/g, more than 50 m²/g, more than about 100 m²/g,more than 100 m²/g, more than about 125 m2/g, and more than 125 m²/g.Additionally or alternatively, the term “reinforcing filler” is used torefer to a particulate material that has a particle size of about 10 nmup to about 1000 nm, including 10 nm up to 1000 nm, about 10 nm up toabout 50 nm, and 10 nm up to 50 nm.

In certain embodiments of the first-third embodiments, the sealantcomposition includes at least one filler selected from: carbon black,silica, clay, starch, calcium carbonate, lignin, a metal oxide, or acellulose ester. Carbon black fillers and silica fillers are discussedin more detail below. In certain embodiments of the first-thirdembodiments, the at least one filler comprises (includes) or consists ofat least one biofiller; non-limiting examples of biofillers (i.e.,fillers that are not sourced from petroleum products or ingredients)include starch, silica, clay, calcium carbonate, lignin, metal oxides,cellulose, cellulose esters, and combinations thereof. Various sourcesexist for the foregoing biofillers, including plant sources of celluloseand lignin, silica from rice hull ash, and silica or carbon black fromplant bagasse. In certain embodiments of the first-third embodiments,the biofiller is added to the sealant composition already incorporatedinto the biorubber (e.g., as an inherent part of the biorubber);non-limiting examples of such biorubber+filler combinations includeguayule rubber containing inherent cellulose from the guayule plantbagasse. In certain embodiments of the first-third embodiments disclosedherein, the sealant composition includes at least one filler comprisingcarbon black. In certain embodiments of the first-third embodimentsdisclosed herein, the filler of the sealant composition consists of oneor more carbon blacks.

Non-limiting examples of suitable fillers for use in the sealantcompositions of certain embodiments of the first-third embodimentsdisclosed herein include, but are not limited to, carbon black, silica,starch, lignin, cellulose ester, talc, clay, boron nitride, aluminumnitride, titanium dioxide, reinforcing zinc oxide, alumina (Al₂O₃),aluminum hydrate (Al₂O₃H₂O), aluminum hydroxide (Al(OH)₃), aluminumcarbonate (Al₂(CO₃)₂), aluminum nitride, aluminum magnesium oxide(MgOAl₂O₃), pyrofilite (Al₂O₃.4SiO₂.H₂O), bentonite (Al₂O₃.4SiO₂.2H₂O),boron nitride, mica, kaolin, glass balloon, glass beads, calcium oxide(CaO), calcium hydroxide (Ca(OH)₂), calcium carbonate (CaCO₃), magnesiumcarbonate, magnesium hydroxide (MH(OH)₂), magnesium oxide (MgO),magnesium carbonate (MgCO₃), titanium oxide, titanium dioxide, potassiumtitanate, barium sulfate, zirconium oxide (ZrO₂), zirconium hydroxide[Zr(OH)₂.nH₂O], zirconium carbonate [Zr(CO₃)₂], crystallinealuminosilicates, and combinations thereof.

Among the useful carbon blacks for use as a filler in certainembodiments of the first-third embodiments disclosed herein are furnaceblack, channel blacks, lamp blacks, and combinations thereof. Morespecifically, examples of useful carbon blacks for use as a filler incertain embodiments of the first-third embodiments disclosed hereininclude super abrasion furnace (SAF) blacks, high abrasion furnace (HAF)blacks, fast extrusion furnace (FEF) blacks, fine furnace (FF) blacks,intermediate super abrasion furnace (ISAF) blacks, semi-reinforcingfurnace (SRF) blacks, medium processing channel blacks, hard processingchannel blacks and conducting channel blacks. Other carbon blacks whichcan be utilized include acetylene blacks. In certain embodiments of thefirst-third embodiments disclosed herein, the sealant compositionincludes a mixture of two or more of the foregoing blacks. Typicalsuitable carbon blacks for use in certain embodiments of the first-thirdembodiments disclosed herein are N-110, N-220, N-339, N-330, N-351,N-550, and N-660, as designated by ASTM D-1765-82a, which one of skillin the art will understand are reinforcing carbon blacks. According tothe first-third embodiments disclosed herein, the carbon blacks utilizedcan be in pelletized form or an unpelletized flocculent mass;preferably, for more uniform mixing, unpelletized carbon black ispreferred. Non-reinforcing carbon black fillers can alternatively oradditionally be utilized as a filler in certain embodiments of thefirst-third embodiments. Non-limiting examples of non-reinforcing carbonblacks for use as a filler in certain embodiments of the first-thirdembodiments disclosed herein include, but are not limited to, thermalblacks or the N9 series carbon blacks (also referred to as the N-900series), such as those with the ASTM designation N-907, N-908, N-990,and N-991. Various carbon blacks meeting the foregoing are commerciallyavailable, including but not limited to Thermax® N990 carbon black fromCancarb Limited (Medicine Hat, Alberta, Canada). In certain embodimentsof the first-third embodiment, when the sealant composition includescarbon black, the carbon black comprises a recycled carbon black;optionally having one of the foregoing ASTM grades. Recycled carbonblack can be sourced from recycled or ground tires.

Non-limiting examples of silica fillers suitable for use in the sealantcompositions of certain embodiments of the first-third embodimentsdisclosed herein include, but are not limited to, precipitated amorphoussilica, wet silica (hydrated silicic acid), dry silica (anhydroussilicic acid), fumed silica, calcium silicate and the like. Othersuitable reinforcing silica fillers for use in sealant compositions ofcertain embodiments of the first-third embodiments disclosed hereininclude, but are not limited to, aluminum silicate, magnesium silicate(Mg₂SiO₄, MgSiO₃ etc.), magnesium calcium silicate (CaMgSiO₄), calciumsilicate (Ca₂SiO₄ etc.), aluminum silicate (Al₂SiO₅, Al₄.3SiO₄.5H₂Oetc.), aluminum calcium silicate (Al₂O₃.CaO₂SiO₂, etc.), and the like.Among the listed reinforcing silica fillers, precipitated amorphouswet-process, hydrated silica fillers are preferred. Such reinforcingsilica fillers are produced by a chemical reaction in water, from whichthey are precipitated as ultrafine, spherical particles, with primaryparticles strongly associated into aggregates, which in turn combineless strongly into agglomerates. The surface area, as measured by theBET method, is a preferred measurement for characterizing thereinforcing character of different reinforcing silica fillers. Incertain embodiments of the first-third embodiments disclosed herein, thesealant composition comprises a reinforcing silica filler having asurface area (as measured by the BET method) of about 32 m²/g to about400 m²/g (including 32 m²/g to 400 m²/g), with the range of about 100m²/g to about 300 m²/g (including 100 m²/g to 300 m²/g) being preferred,and the range of about 150 m²/g to about 220 m²/g (including 150 m²/g to220 m²/g) being included. In certain embodiments of the first-thirdembodiments disclosed herein, the sealant composition comprisesreinforcing silica filler having a pH of about 5.5 to about 7 orslightly over 7, preferably about 5.5 to about 6.8. Some of thecommercially available reinforcing silica fillers which can be used inthe sealant compositions of certain embodiments of the first-thirdembodiments disclosed herein include, but are not limited to, Hi-Sil®190, Hi-Sil® 210, Hi-Sil® 215, Hi-Sil® 233, Hi-Sil® 243, and the like,produced by PPG Industries (Pittsburgh, Pa.). As well, a number ofuseful commercial grades of different reinforcing silica fillers arealso available from Degussa Corporation (e.g., VN2, VN3), Rhone Poulenc(e.g., Zeosil™ 1165 MP), and J. M. Huber Corporation.

Cure Package

In certain embodiments of the first-third embodiments disclosed herein,the sealant composition includes a cure package. The ingredients of thecure package allow the sealant composition to “cure” the composition,thereby cross-linking molecular chains of the biorubber. Although thecure package can be understood as enabling curing of the sealantcomposition, the sealant composition will generally remain tacky orsticky even after curing. According to those embodiments of thefirst-third embodiments disclosed herein, when the sealant compositionincludes a cure package, the particular ingredients of the cure packagemay vary. In certain embodiments of the first-third embodimentsdisclosed herein, the cure package will include at least one vulcanizingagent and at least one vulcanizing accelerator; in certain suchembodiments, the cure package also includes at least one vulcanizationactivator (e.g., zinc oxide, stearic acid, and the like) and optionallyat least one vulcanization inhibitor. Notably, one or more than one ofeach of the foregoing can be utilized (e.g., one or more than onevulcanizing accelerator). In certain embodiments of the first-thirdembodiments, the cure package will include a vulcanizing agent; avulcanizing accelerator; a vulcanizing activator (e.g., zinc oxide,stearic acid, and the like); a vulcanizing inhibitor, and ananti-scorching agent. Notably, one or more than one of each of theforegoing can be utilized (e.g., one or more than one vulcanizingaccelerator). In certain embodiments of the first-third embodiments, thecure package includes at least one vulcanizing agent, at least onevulcanizing accelerator, at least one vulcanizing activator, andoptionally a vulcanizing inhibitor and/or an anti-scorching agent.Vulcanizing accelerators and vulcanizing activators act as catalysts forthe vulcanization agent. Vulcanizing inhibitors and anti-scorchingagents are known in the art and can be selected by one skilled in theart based on the vulcanizate properties desired. When amounts of variousingredients of a cure package are discussed below as phr, the term isintended to refer to the parts per 100 parts of biorubber. In certainembodiments of the first-third embodiments, the cure package comprisesabout 2 to about 15% by weight of the sealant composition, including2-15% by weight (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15%by weight), 2-12% by weight, 2-10% by weight, 4-15% by weight, 4-12% byweight, 4-10% by weight, 5-12% by weight, and 5-10% by weight.

Examples of suitable types of vulcanizing agents for use in the sealantcompositions according to certain embodiments of the first-thirdembodiments, include but are not limited to, sulfur or peroxide-basedcuring components. Thus, in certain such embodiments, the curativecomponent includes a sulfur-based curative or a peroxide-based curative.Examples of specific suitable sulfur vulcanizing agents include“rubbermaker's” soluble sulfur; sulfur donating curing agents, such asan amine disulfide, polymeric polysulfide, or sulfur olefin adducts; andinsoluble polymeric sulfur. Preferably, the sulfur vulcanizing agent issoluble sulfur or a mixture of soluble and insoluble polymeric sulfur.For a general disclosure of suitable vulcanizing agents and othercomponents used in curing, e.g., vulcanizing inhibitor andanti-scorching agents, one can refer to Kirk-Othmer, Encyclopedia ofChemical Technology, 3rd ed., Wiley Interscience, N.Y. 1982, Vol. 20,pp. 365 to 468, particularly Vulcanization Agents and AuxiliaryMaterials, pp. 390 to 402, or Vulcanization by A. Y. Coran, Encyclopediaof Polymer Science and Engineering, Second Edition (1989 John Wiley &Sons, Inc.), both of which are incorporated herein by reference.Vulcanizing agents can be used alone or in combination. In certainembodiments of the first-third embodiments, the vulcanizing agent ispresent in the sealant composition in an amount ranging from 0.1 to 10phr (i.e., based upon 100 parts of the biorubber), including from 0.1 to7.5 phr, including from 0.1 to 5 phr, and preferably from 0.1 to 3.5phr.

In certain embodiments of the first-third embodiments disclosed herein,the sealant composition includes at least one vulcanizing accelerator.Vulcanizing accelerators are used to control the time and/or temperaturerequired for vulcanization (or curing) and to improve properties of theresulting composition. According to the first-third embodimentsdisclosed herein, the type and amount of vulcanization accelerator(s)used in the sealant composition may vary. In certain embodiments of thefirst-third embodiments disclosed herein, the at least one vulcanizationaccelerator is selected from at least one of the following classes ofvulcanization accelerators: thiurams, thioureas, dithiocarbamates,xanthates, or thiophosphates. In certain embodiments of the first-thirdembodiments, the at least one vulcanization accelerator comprises athiazole, optionally in combination with one of more vulcanizationaccelerators from one or more of the foregoing classes. Non-limitingexamples of vulcanizing accelerators that belong to the class ofthiurams include: TMTM (tetramethyl thiuram monosulfide), TMTD(tetramethyl thiuram disulfide), DPTT (dipentamethylene thiuramtetrasulfide), TETD (tetraethyl thiuram disulfide), TiBTD (tetraisobutylthiuram disulfide), and TBzTD (tetrabenzyl thiuram disulfide).Non-limiting examples of vulcanizing accelerators that belong to theclass of thioureas include: ETU (ethylene thiourea), DPTU (N,N-diethylthiourea), DETU (N,N-dibutylthiourea), and DBTU (diphenyl thiourea).Non-limiting examples of vulcanizing accelerators that belong to theclass of dithiocarbamates include: ZDMC (zinc dimethyl dithiocarbamate),ZDEC (zinc diethyl dithiocarbamate), ZDBC (zinc dibutyldithiocarbamate), ZEDC (zinc N-ethyl-dithiocarbamate), CDMC (copperdimethyl dithiocarbamate) and ZBEC (zinc dibenzyl dithiocarbamate).Non-limiting examples of vulcanizing accelerators that belong to theclass of xanthates include: ZIX (zinc isopropyl xanthate). Non-limitingexamples of vulcanizing accelerators that belong to the class ofthiophosphates include: ZBDP (Zinc-O,O-di-N-phosphorodithioate).Non-limiting examples of vulcanizing accelerators that belong to theclass of thiazoles incluee: MBT (2-mercaptobenzothiazole), MBTS(2,2-benzothiazole disulfide), ZMBT (zinc 2-mercaptobenzothiazole) andCMBT (copper 2-mercaptobenzothiazole). Additional examples of suitablevulcanizing accelerators for use in certain embodiments of thefirst-third embodiments disclosed herein include, but are not limitedto, sulfonamides (e.g., N-cyclohexyl-2-benzothiazole-sulfenamide (CBS),N-tert-butyl-2-benzothiazole-sulfenamide (TBBS), and the like);guanidine vulcanization accelerators (e.g., diphenyl guanidine (DPG) andthe like); and carbamate vulcanizing accelerators (e.g., zinc dibutyldithocarbamate (ZDBC), zinc dibenzyl dithiocarbamate (ZBEC), zincdiethyl dithiocarbamate (ZDEC), zinc dimethyl dithiocarbamate (ZDMC),zinc N-ethyl-dithiocarbamate (ZEDC), copper dimethyl diothiocarbmate(CDMC), and the like), and combinations thereof; such vulcanizationaccelerators can be used either alone, in combination, or in combinationwith one of the foregoing classes of vulcanization accelerators.Generally, the total amount of vulcanization accelerator used rangesfrom 0.5 to 20 phr, 0.5 to 15 phr, 1 to 15 phr, or 2 to 10 phr.

Vulcanizing activators are additives that can be used to supportvulcanization. According to embodiments of the first-third embodiments,vulcanizing activators will generally include both an inorganic andorganic component. Zinc oxide is the most widely used inorganicvulcanization activator. Various organic vulcanization activators arecommonly used including stearic acid, palmitic acid, lauric acid, andzinc salts of each of the foregoing. In certain embodiments of thefirst-third embodiments, the total amount of vulcanization activatorused ranges from 0.1 to 20 phr, 0.5 to 15 phr, or 1 to 15 phr. Incertain embodiments of the first-third embodiments the vulcanizationactivator comprises zinc oxide in an amount of 1 to 15 phr, 2 to 10 phr,or 5 to 10 phr. In certain embodiments of the first-third embodiments,the vulcanization accelerator comprises stearic acid in an amount of 0.1to 6 phr, 0.5 to 5 phr, or 1 to 4 phr.

Vulcanization inhibitors that can be used to control the vulcanizationprocess and generally retard or inhibit vulcanization until the desiredtime and/or temperature is reached. In certain embodiments of thefirst-third embodiments, the vulcanization inhibitor includes PVI(cyclohexylthiophthalmide) from Santogard. In certain embodiments of thefirst-third embodiments, the amount of vulcanization inhibitor is 0.1 to3 phr, preferably 0.5 to 2 phr.

Methods for Preparing the Sealant Composition

Various mixing methods can be used for combining the ingredients of thesealant composition. In certain embodiments, the sealant composition isprepared by a process that comprises: providing ingredients includingbiorubber, softener (i.e., plant resin and/or plant oil), and anyfiller, and mixing to form a masterbatch which results in the sealantcomposition. In certain such embodiments, a final batch is prepared fromthe masterbatch by adding the cure package ingredients thereto andmixing, resulting in the final sealant composition.

In certain embodiments, more than one masterbatch stage may be utilized,e.g., an initial masterbatch followed by a secondary masterbatch or aremill mixing step, particularly when relatively higher amounts offiller(s) are used. The foregoing process options may also (optionally)be utilized in preparing the sealant composition of the first embodimentas well as in preparing the sealant composition for use in the secondand third embodiments.

The preparation of the masterbatch(es) and the final batch may generallyinvolve mixing together the ingredients for the sealant composition (asdisclosed above) by methods known in the art, such as, for example, bykneading the ingredients together in a Banbury mixer, kneader, or on amilled roll. The term masterbatch as used herein is intended to refer toa non-productive mixing stage, which is known to those of skill in theart and generally understood to be a mixing stage where no vulcanizingagents or vulcanization accelerators are added. The term final batch asused herein is intended to refer to a productive mixing stage, which isalso known to those of skill in the art and generally understood to bethe mixing stage where the vulcanizing agents and vulcanizationaccelerators are added into the sealant composition.

In certain embodiments, the sealant composition of the first-thirdembodiments is prepared by a process including a master batch mixingstage(s) conducted at a temperature of about 80° C. to about 150° C.(e.g., 80, 90, 100, 110, 120, 130, 140 or 150° C.). In certainembodiments, the sealant composition of the first-third embodiments isprepared by a process that also includes a final mixing stage conductedat a temperature below the vulcanization temperature in order to avoidunwanted pre-cure of the sealant composition. Therefore, the temperatureof the productive (or final) mixing stage should not exceed about 160°C. (e.g., 80, 90, 100, 110, 120, 130, 140, 150, 160° C.) and istypically about 80° C. to about 150° C. In certain embodiments, thesealant composition of the first-third embodiments is prepared by aprocess including at least two master batch mixing stages (which may beconducted at the foregoing temperature) wherein at least a majority(e.g., (at least) 51 weight %, (at least) 55 weight %, (at least) 60weight %, (at least) 65 weight %, (at least) 70 weight %, (at least) 75weight %, (at least) 80 weight %, (at least) 85 weight %, (at least) 90weight %, (at least) 95 weight %, (at least) 98 weight %) by weight ofany plant oil is added in the second master batch mixing stage; incertain such embodiments, the second master batch mixing stage for atleast a majority of oil is only utilized when at least 30 phr of oil(e.g., 30 phr, 40 phr, 50 phr, 60 phr, 70 phr, 80 phr, 90 phr, 100 phror more) is used in the sealant composition.

Tires

As discussed above, according to the second embodiment disclosed herein,a tire comprising at least one component in contact with a sealantcomposition according to the first embodiment is disclosed. In otherwords, the second embodiment disclosed herein should be understood asbeing directed to a tire comprising at least one component in contactwith a sealant composition wherein the sealant composition has acomposition as described above. According to certain embodiments of thesecond embodiment, the tire comprises at least one of the followingcomponents: a tread, one or more body/carcass plies, one or more capplies, one or more belt plies, a sidewall, or an air barrier. As usedherein, the term “air barrier” should be understood as includingtraditional type innerliners (e.g., a rubber layer made of butyl and/orhalogenated-butyl rubber) as well non-traditional innerliners (e.g.,spray-on, paint-on, films made of plastics or polymers other than butylrubber, or a press-on type innerliner with removable film backing). Incertain embodiments of the second embodiment, the tire component incontact with the sealant composition comprises or consists of aninnerliner, optionally an innerliner comprising a rubber layer made ofbutyl and/or halogenated butyl rubber (which rubber layer may be wrappedaround the annual beads of the sidewalls of the tire). In certainembodiments of the second embodiment, the tire component in contact withthe sealant composition comprises or consists of a body ply. As usedherein, the term “body ply” refers to a rubber ply wrappedcircumferentially around the tire and extending from one annual bead tothe other. As used herein, the term “carcass ply” is used to refer to atype of body ply positioned radially inward of the tread, extending frombead to bead, and generally comprises a layer of rubber-covered textilecords. The cords of the carcass ply may be positioned radially ordiagonally (i.e., not circumferentially). When more than one carcass plyis utilized, each may be positioned such that their cord directiondiffers (e.g., biased to each other). As used herein, the term “beltply” refers to one or more layers of rubber-covered steel cord generallypositioned radially inward of the tread but radially outward of any bodyor carcass plies. In certain embodiments of the second embodiment, thetire contains sealant composition positioned between the inner liner andthe body ply. In certain embodiments of the second embodiment where thetire component in contact with the sealant composition comprises orconsists of an innerliner (optionally an innerliner comprising a rubberlayer made of butyl and/or halogenated butyl rubber which rubber layermay be wrapped around the annual beads of the sidewalls of the tire),the sealant composition is positioned on the radially inward surface ofthe innerliner.

According to the second embodiment, the sealant composition may beapplied to at least one component of the tire according to variousmethods. Non-limiting examples of those methods include the methods ofthe third embodiment, as discussed below. Generally, any method whichenables the sealant composition to contact at least one component of thetire can be utilized. In certain embodiments of the second embodiment,any method which enables the sealant composition to at least partiallycoat at least one surface of the tire component can be utilized. Incertain embodiments of the second embodiment, the sealant compositioncoats or covers at least a majority of at least one surface of the tirecomponent and is applied thereto from bead to bead or from belt edge tobelt edge. In certain embodiments of the second embodiment, the sealantcomposition coats or covers at least 60%, at least 70%, at least 80%, atleast 90%, at least 95%, at least 98%, at least 99% or even 100% of atleast one surface of the tire component and is applied from bead to beador from belt edge to belt edge. Preferably, the at least one surface ofthe tire component comprises the radially inward surface of that tirecomponent.

Methods for Applying Sealant Composition to Tire Components

As discussed above, according to the third embodiment disclosed herein,a method for applying a sealant composition to a tire is disclosed. Themethod comprises: providing a tire comprising at least one of thefollowing components: a tread, one or more body or carcass plies, one ormore cap plies, one or more belt plies, a sidewall, or an air barrierlayer; and applying a sealant composition according to the firstembodiment to a portion of at least one radially inner surface, aportion of at least one radially outer surface, or portions of bothradially inner and radially outer surfaces.

In certain embodiments of the third embodiment, the tire is cured priorto applying the sealant composition. In certain embodiments of the thirdembodiment, the tire is cured prior to applying the sealant compositionand an air barrier layer is added to the tire after applying the sealantcomposition to the cured tire; in certain such embodiments, the airbarrier layer is a non-traditional inner liner (e.g., spray-on,paint-on, films made of plastics or polymers other than butyl rubber, ora press-on type innerliner with removable film backing). In certainembodiments of the third embodiment, the sealant composition is appliedto the component of the tire so that it is positioned between the bodyply and innerliner.

According to the third embodiment disclosed herein, the particularmethod by which the sealant composition is applied to at least a portionof the surface of at least one component of the tire is not particularlylimited. In certain embodiments of the third embodiment, the applying ofthe sealant composition comprises at least one of: painting, pouring,spraying, or pressing. According to certain embodiments of theforegoing, the sealant composition may be calendered into a layer priorto applying to the tire component. In certain embodiments of the thirdembodiment, the sealant composition is combined with a removable backingenabling the sealant composition side to be applied to the tirecomponent followed by removal of the backing material.

According to the third embodiment disclosed herein, the temperature ofthe sealant composition when applied to the tire component may vary. Incertain embodiments of the third embodiment, the sealant composition isheated above room temperature (i.e., above 25° C.) prior to beingapplied to the tire component; in certain such embodiments, the sealantcomposition is heated to a temperature of about 50 to about 150° C.(e.g., 50° C., 60° C., 70° C., 80° C., 90° C., 100° C., 105° C., 110°C., 115° C., 120° C., 125° C., 130° C., 135° C., 140° C., 145° C., or150° C.), including about 60 to about 140° C., and 60-140° C. As thoseof skill in the art will appreciate, when heating the sealantcomposition prior to application to the tire component, a temperaturethat cause the sealant composition to scorch should be avoided. Theparticular temperature at which the sealant composition will scorch willdepend upon the particular ingredients selected (e.g., the biorubber(s),plant resin(s) and/or plant oil(s), and cure package). The foregoingtemperatures refer to the temperature to which the sealant compositionis heated (e.g., as could be determined by a temperature probe insertedinto a container of the heated sealant composition). Preferably, whenthe sealant composition is heated prior to being applied to the tirecomponent, the maximum temperature of heating will be less than thescorch temperature of the sealant composition. In certain embodiments ofthe third embodiment, the sealant composition is heated to one of theforegoing temperatures and maintained (or held) at such temperature fora period of time such as about 5 minutes to about 1 hour (e.g., 5minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 40minutes, 45 minutes, 50 minutes, or 1 hour), preferably about 15 minutesto about 40 minutes; in certain such embodiments during the time thatthe sealant composition is maintained or held at one of the foregoingtemperatures it is mixed or otherwise agitated. Heating the sealantcomposition to a relatively higher temperature above room temperature(e.g., at least 100° C.) may eliminate the need to hold the sealantcomposition at an elevated temperature for one of the foregoing timeperiods.

EXAMPLES

The following examples illustrate specific and exemplary embodimentsand/or features of the embodiments of the present disclosure. Theexamples are provided solely for the purposes of illustration and shouldnot be construed as limitations of the present disclosure. Numerousvariations over these specific examples are possible without departingfrom the spirit and scope of the presently disclosed embodiments. Itshould specifically be understood that the particular softener utilizedin the examples can be utilized with biorubbers, fillers, and otheringredients each of which differ in amount, composition, or both fromthose used in the examples (i.e., as fully disclosed in the precedingparagraphs).

Example 1

A sealant composition was prepared using the ingredients listed inTable 1. The polyfarnesene used for the biorubber was obtained fromKuraray Co., Ltd, and had a molecular weight (Mw) of 135 kD(kilo-Daltons), a Tg of −71° C., and a viscosity (at 38° C.) of 69 Pa*s.The filler utilized was carbon black, more specifically a N300 seriesreinforcing carbon black. The softener utilized was guayule resin. Thenon-petroleum content of the sealant composition was 80 weight % (basedupon the total weight of the sealant composition and without includingthe stearic acid as a non-petroleum ingredient). The amounts provided inTable 1 can be understood in terms of parts or phr (e.g., the non-rubberingredients are listed based upon 100 parts of biorubber).

TABLE 1 Ingredient Amount (phr) Polyfarnesene 100 Carbon black 16Guayule resin 30 Vulcanizing agent (sulfur) 0.6 Vulcanization activator#1 2.4 (Stearic acid) Vulcanization activator #2 8.4 (Zinc oxide)Vulcanization accelerator 4.2 (TBzTD)

In order to prepare the sealant composition, the ingredients of Table 1were mixed according to the procedure provided in Table 2, using amixer.

TABLE 2 Mixing Parameters Stage Time (total) Condition Masterbatch  0seconds Charge polymer(s). Stage 1 (initial 30 seconds Charge carbonblack and resin in amounts as temp: 90° C., indicated in Table 1,maintain rotor at 60 rpm and rotor rpm temperature at 90° C. started at60) Final Batch 60 seconds Charge curatives while maintaining rotor at60 rpm Stage (initial and temperature at 90° C. temp. 90° C.) 1800seconds  Raise temperature to 130° C., reduce rotor speed to 30 rpm andmaintain temperature at 130° C., drop at end of time.

The viscosity of the sealant composition of Example 1 can be measured asa real dynamic viscosity, and determined using an Alpha Technologies RPA(Rubber Process Analyzer) instrument which is rotorless. Measurementscan be made following the guidance of, but not strictly according toASTM D 6204, and in accordance with ASTM D 6204, a three point frequencysweep can be conducted. The rubber compositions may be pre-heated for 1minute at 100° C. and in accordance with the ASTM procedure, a strainsweep can be conducted at 100° C., strain at 50 percent, 1 Hz, and 1minute. Viscosity data can be reported from a run conducted at 266° F.,G′ at 0.2 minutes.

Examples 2 and 3

A sealant composition is prepared using the ingredients listed in Table3. A guayule rubber as the biorubber is obtained from a pilot processingand has a molecular weight (Mw) of 1.3 million grams/mole a Mn of about450,000 grams/mole (by GPC using a polystyrene standard), a Tg of −60°C., and a ML(1+4) Mooney viscosity of 95. The polyfarnesene is asdescribed in Example 1. The filler utilized is carbon black, morespecifically a N300 series reinforcing carbon black. The softenerutilized is soybean oil from Archer Daniels Midland (ADM). Thenon-petroleum content of the sealant composition is listed below inweight % (based upon the total weight of the sealant composition). Theamounts provided in Table 3 can be understood in terms of parts or phr(e.g., the non-rubber ingredients are listed based upon 100 parts ofbiorubber). In order to prepare the sealant compositions of Examples 2and 3, the ingredients of Table 3 are mixed according to the sameprocedure as provided in Table 2 above. Since relatively more of thepolyfarnesene is utilized in Example 3 as compared to Example 2 theamount of soybean oil was lowered to 200 phr from 300 phr.

TABLE 3 Amount (phr) Amount (phr) Ingredient Example 2 Example 3 Guayulenatural rubber 80 60 Polyfarnesene 20 40 Carbon black 20 20 Soybean oil300 200 Guayule resin 20 20 Vulcanizing agent (sulfur) 1 1 Vulcanizationactivator #1 (Stearic 3 3 acid) Vulcanization activator #2 (Zinc oxide)10 10 Vulcanization accelerator (TBzTD) 5 5 Total parts 459 359 % byweight non-petroleum 92 89

This application discloses several numerical range limitations thatsupport any range within the disclosed numerical ranges, even though aprecise range limitation is not stated verbatim in the specification,because the embodiments of the compositions and methods disclosed hereincould be practiced throughout the disclosed numerical ranges. Withrespect to the use of substantially any plural or singular terms herein,those having skill in the art can translate from the plural to thesingular or from the singular to the plural as is appropriate to thecontext or application. The various singular or plural permutations maybe expressly set forth herein for sake of clarity.

It will be understood by those within the art that, in general, termsused herein, and especially in the appended claims are generallyintended as “open” terms. For example, the term “including” should beinterpreted as “including but not limited to,” the term “having” shouldbe interpreted as “having at least,” the term “includes” should beinterpreted as “includes but is not limited to.” It will be furtherunderstood by those within the art that if a specific number of anintroduced claim recitation is intended, such an intent will beexplicitly recited in the claim, and in the absence of such recitationno such intent is present. For example, as an aid to understanding, thefollowing appended claims may contain usage of the introductory phrases“at least one” and “one or more” to introduce claim recitations.However, the use of such phrases should not be construed to imply thatthe introduction of a claim recitation by the indefinite articles “a” or“an” limits any particular claim containing such introduced claimrecitation to inventions containing only one such recitation, even whenthe same claim includes the introductory phrases “one or more” or “atleast one” and indefinite articles such as “a” or “an” (e.g., “a” or“an” should typically be interpreted to mean “at least one” or “one ormore”); the same holds true for the use of definite articles used tointroduce claim recitations. In addition, even if a specific number ofan introduced claim recitation is explicitly recited, those skilled inthe art will recognize that such recitation should typically beinterpreted to mean at least the recited number (e.g., the barerecitation of “two recitations,” without other modifiers, typicallymeans at least two recitations, or two or more recitations).Furthermore, in those instances where a convention analogous to “atleast one of A, B, and C, etc.” is used, in general such a constructionis intended in the sense one having skill in the art would understandthe convention (e.g., “a system having at least one of A, B, and C”would include but not be limited to systems that have A alone, B alone,C alone, A and B together, A and C together, B and C together, and/or A,B, and C together, etc.). It will be further understood by those withinthe art that virtually any disjunctive word or phrase presenting two ormore alternative terms, whether in the description, claims, or drawings,should be understood to contemplate the possibilities of including oneof the terms, either of the terms, or both terms. For example, thephrase “A or B” will be understood to include the possibilities of “A”or “B” or “A and B.”

All references, including but not limited to patents, patentapplications, and non-patent literature are hereby incorporated byreference herein in their entirety.

While various aspects and embodiments of the compositions and methodshave been disclosed herein, other aspects and embodiments will beapparent to those skilled in the art. The various aspects andembodiments disclosed herein are for purposes of illustration and arenot intended to be limiting, with the true scope and spirit beingindicated by the claims.

What is claimed is:
 1. A tire comprising at least one component incontact with a sealant composition comprising biorubber in an amount ofabout 15 to about 90 weight %, based upon the total weight of thesealant composition; and a softener comprising at least one of plantresin or plant oil, in an amount of about 10 to about 85 weight %, basedupon the total weight of the sealant composition, and optionally a curepackage, wherein the sealant composition contains no more than 5% byweight water, based upon the total weight of the sealant composition,and contains at least 70 weight %, based upon the total weight of thesealant composition, non-petroleum ingredients including the biorubber,and plant resin or plant oil, and the sealant composition has aviscosity of 200 to 500 Pa-S at 100° C.
 2. The tire of claim 1 whereinthe sealant composition further comprises at least one filler in anamount of up to 20 weight %, based upon the total weight of the sealantcomposition.
 3. The tire of claim 1, wherein the softener comprises aplant resin, the plant resin is present in an amount of 10 to 45 weight%, based upon the total weight of the sealant composition, and thebiorubber:plant resin weight ratio is greater than 1:1.
 4. The tire ofclaim 1, wherein the softener comprises a plant oil.
 5. The tire ofclaim 1, wherein the biorubber comprises at least one of polyfarnesene,non-Hevea natural rubber, Hevea natural rubber, or a polymer orcopolymer comprising at least one conjugated diene-containingnon-petroleum monomer optionally in combination with at least onearomatic vinyl non-petroleum monomer.
 6. The tire of claim 1, whereinthe softener comprises a plant resin comprising guayule resin, coniferresin, citrus resin, or a combination thereof.
 7. The tire of claim 6,wherein the plant resin comprises at least one terpene, at least oneargentatin, at least one guayulin, or a combination thereof.
 8. The tireof claim 1, wherein the biorubber comprises polyfarnesene having amolecular weight (Mw) of less than 500,000 kDa.
 9. The tire of claim 1,wherein the composition meets at least one of the following: a. has aviscosity of about 300 to about 400 Pa-S at 100° C., b. contains no morethan 25% by weight of an elastomer/rubber that is solid at roomtemperature, based upon the total weight of the sealant composition, c.contains 10 to 70% by weight oil, based upon the total weight of thesealant composition, d. the cure package is present and comprises about2 to about 15 weight %, based upon the total weight of the sealantcomposition; e. carbon black is present as filler; or f. the softenercomprises guayule resin.
 10. The tire of claim 9, wherein each of(a)-(f) is met.
 11. The tire of claim 1, wherein the biorubber isextended with at least a portion of the plant resin and/or plant oil.12. The tire of claim 1, wherein the biorubber comprises polyfarnesenein an amount of about 50 to about 70 weight %, based upon the totalweight of the sealant composition, and the softener comprises guayuleresin in an amount of about 10 to about 30% by weight, based upon thetotal weight of the sealant composition.
 13. The tire of claim 1,wherein the biorubber comprises polyfarnesene in an amount of about 50to about 70 weight %, based upon the total weight of the sealantcomposition, and the softener comprises guayule resin in an amount ofabout 10 to about 30% by weight, based upon the total weight of thesealant composition.
 14. The tire of claim 1, wherein the sealantcomposition further comprises at least one filler in an amount of up to20 weight %, based upon the total weight of the sealant composition. 15.The tire of claim 14, wherein the at least one filler is selected fromthe group consisting of carbon black, silica, clay, starch, calciumcarbonate, lignin, metal oxidex, and cellulose ester.
 16. The tire ofclaim 1, wherein the at least one component comprises an inner liner ora body ply having at least one surface at least partially coated withthe sealant composition.
 17. A tire comprising at least one component incontact with a sealant composition comprising biorubber in an amount ofabout 15 to about 80 weight %, based upon the total weight of thesealant composition; and a softener comprising at least one of plantresin or plant oil, in an amount of about 20 to about 85 weight %, basedupon the total weight of the sealant composition, at least one filler inan amount of up to 20 weight %, based upon the total weight of thesealant composition, and a cure package, wherein the sealant compositioncontains no more than 5% by weight water, based upon the total weight ofthe sealant composition, and contains at least 90 weight %, based uponthe total weight of the sealant composition, non-petroleum ingredientsincluding the biorubber, and plant resin or plant oil, and the sealantcomposition has a viscosity of 200 to 500 Pa-S at 100° C.
 18. The tireof claim 17, wherein the softener comprises guayule resin in an amountof about 10 to about 30% by weight, based upon the total weight of thesealant composition.
 19. The tire of claim 17, wherein the biorubbercomprises polyfarnesene in an amount of about 20 to about 40% by weight,based upon the total weight of the biorubber, and the softener comprisesguayule resin in an amount of about 5 to about 20% by weight, based uponthe total weight of the softener.